HygiRelief Procedure and HygiSample Evaluation for Patients Diagnosed With Rome IV Functional Constipation Previously Managed With Linzess
试验速览
- 阶段
- 不适用
- 状态
- 撤回
- 主要终点
- Assess change in bowel movements PRE and POST HygiRelief procedure
研究概览
简要总结
This study has a single center, prospective, open label design. The population will include patients diagnosed with Rome IV Functional Constipation who are at the time of study enrollment being managed with a stable dose of Linzess. They will stop taking their Linzess, undergo monitoring of bowel habits for 2 weeks, have a HygiRelief procedure and then undergo an additional 2 weeks of bowel habit monitoring.
详细描述
After undergoing a 5-7 day Linzess washout period, patients will record their bowel habits in a daily diary for 2 weeks. Patients will have the HygiRelief procedure with a HygiSample evaluation, then they will record their bowel habits in a daily diary for 2 weeks following the HygiRelief procedure.
HygiSamples (stool samples) will be collected throughout the HygiRelief procedure and the samples will be sent for microbiome evaluation.
Patients will complete multiple questionnaires - Happiness Scale, Hospital Anxiety and Depression Scale (HADS), and a personal assessment which includes the Constipation Symptom Score and Adverse Event Screening. These will be completed at Baseline, after the 2 week PRE-HygiRelief period, and after the 2 week POST-HygiRelief period.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 80 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patient's age is between 18 and 80 years old
- •Patient diagnosed with Rome IV Functional Constipation (Attachment C2)
- •Patient is currently managed with Linzess and willing to stop taking it for study duration
排除标准
- •Patient has functional bowel disorders characterized by alternating bowel habits (diarrhea/constipation)
- •Patient has any other condition that, in the opinion of the investigator, may adversely affect the compliance or safety of the patient or would limit the patient's ability to complete the study
- •Patient has any of the contraindications listed below:
- •Cardiac: Congestive heart failure (NYHA class III or IV or EF <50%)
- •GI: Intestinal perforation, carcinoma of the rectum, fissures or fistula, severe hemorrhoids, abdominal hernia, recent colon, rectal, or abdominal surgery
- •GU: Renal insufficiency (CC < 60 ml/min/173m2), cirrhosis with ascites
- •Abdominal surgery within the last 6 months
- •Patient took antibiotics within two months of starting the study
结局指标
主要结局
Assess change in bowel movements PRE and POST HygiRelief procedure
时间窗: 12 months
Evaluate the clinical effectiveness of the HygiRelief procedure to relieve functional constipation in patients previously managed with a stable dose of Lizess
次要结局
- Assess colon effluent samples (HygiSample) collected during the HygiRelief procedure(12 months)